Global biopharmaceutical leader GSK (GlaxoSmithKline) has announced a new opportunity for experienced quality professionals. The company is hiring a Specialist – QAC Audit Intake Coordinator – GCC for its Bengaluru office. Candidates with experience in Quality Assurance (QA), GMP compliance, audit coordination, CAPA management, and pharmaceutical quality systems are encouraged to apply.

This is an excellent opportunity for professionals seeking a Quality Assurance job in Bangalore, particularly those with experience in pharmaceutical audits, supplier quality management, regulatory inspections, and quality operations.

Job Overview

About GSK

GSK is a leading global biopharmaceutical company focused on uniting science, technology, and talent to get ahead of disease together. The organization delivers medicines and vaccines worldwide and operates one of the largest pharmaceutical manufacturing and supply networks globally.

The company’s quality and compliance functions play a critical role in ensuring patient safety, regulatory compliance, and continuous improvement across manufacturing and supplier operations.

Key Responsibilities

The selected candidate will be responsible for managing audit intake workflows and supporting quality assurance activities across GSK’s Global Contract Operations network.

Audit Coordination

• Receive and manage audit requests.
• Confirm audit scope and requirements.
• Assign reviewers and schedule audits.
• Coordinate internal and external quality audits.

Quality Systems Management

• Maintain audit and inspection records.
• Ensure documentation accuracy within quality management systems.
• Support data integrity and compliance activities.
• Maintain audit-related databases and records.

CAPA Tracking

• Monitor corrective and preventive actions (CAPAs).
• Follow up on action items until closure.
• Escalate overdue or critical quality issues.
• Generate CAPA status reports.

Regulatory Inspection Support

• Coordinate logistics for regulatory inspections.
• Assist during internal and external audits.
• Prepare audit documentation packages.
• Support inspection readiness activities.

Reporting & Analytics

• Create quality dashboards and reports.
• Analyze audit trends and compliance metrics.
• Present audit status updates to stakeholders.
• Support risk-based decision-making.

Required Qualifications

Candidates applying for this GSK Quality Assurance job should possess:

• Bachelor’s degree in Pharmacy, Chemistry, Microbiology, Life Sciences, or a related discipline.
• Minimum 3 years of experience in Quality Assurance, Quality Operations, or Audit Coordination.
• Practical knowledge of GMP regulations and pharmaceutical quality systems.
• Strong organizational and project coordination skills.
• Experience managing multiple priorities and deadlines.
• Proficiency in Microsoft Office applications.
• Excellent written and verbal English communication skills.

Preferred Qualifications

Applicants with the following skills will have an advantage:

• Experience with Contract Manufacturing Organizations (CMOs).
• Supplier Quality Management experience.
• CAPA management expertise.
• Root Cause Analysis and investigation skills.
• Regulatory inspection support experience.
• Risk management knowledge.
• Experience using Electronic Quality Management Systems (eQMS).
• Global audit program exposure.

Essential Skills

• Quality Assurance (QA)
• GMP Compliance
• GxP Regulations
• Supplier Auditing
• CAPA Management
• Pharmaceutical Regulatory Compliance
• Risk Assessment
• Data Integrity
• Technical Writing
• Quality Metrics Reporting
• Lean Management
• Stakeholder Communication

Salary Expectation

Based on industry standards for Quality Assurance professionals in Bengaluru, the estimated salary range for this role is:

₹8,00,000 – ₹14,00,000 per annum (CTC)

Actual compensation may vary depending on experience, qualifications, and internal company policies.

Why Join GSK?

Working at GSK offers professionals an opportunity to:

• Contribute to global healthcare innovation.
• Work with world-class quality systems.
• Gain exposure to international regulatory standards.
• Collaborate with global cross-functional teams.
• Build expertise in pharmaceutical audits and compliance.
• Enjoy a flexible hybrid work model.
• Access career growth opportunities in a leading biopharma organization.

How to Apply

Application Link